Canonical Allele Identifier: CA453967836
Gene: DNAH11 HGNC NCBI

Linked Data

dbSNP Id: rs765976416
MyVariant Identifiers: chr7:g.21920325A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.21880707A>G , CM000669.2:g.21880707A>G GRCh38
NC_000007.13:g.21920325A>G , CM000669.1:g.21920325A>G GRCh37
NC_000007.12:g.21886850A>G NCBI36
NG_012886.2:g.342493A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409508.8:c.12201A>G MANE Select ENSP00000475939.1:p.Thr4067=
ENST00000328843.10:c.12222A>G ENSP00000330671.7:p.Thr4074=
ENST00000409508.7:c.12201A>G ENSP00000475939.1:p.Thr4067=
ENST00000620169.4:c.12222A>G ENSP00000481693.1:p.Thr4074=
NM_001277115.1:c.12201A>G NP_001264044.1:p.Thr4067=
NM_001277115.2:c.12201A>G MANE Select NP_001264044.1:p.Thr4067=